Clinical Research Study Coordinator
Core
Run all aspects of assigned clinical trials, including IRB submissions, patient recruitment, and protocol adherence.
Role type
Clinical Research Study Coordinator
Builds
Clinical trial operations and regulatory compliance
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Clinical trial execution, IRB submission management, patient recruitment and screening, protocol implementation, regulatory document management, adverse event reporting, data entry and query resolution, quality assurance, problem solving, organization
Preferred skills
Nursing degree, Oncology focus
Technologies
Electronic databases, patient input databases
Responsibilities
Prepare and coordinate study submissions to IRB and committees; communicate with study staff, IRB, sponsors, and investigators; prepare informed consent forms; maintain regulatory documents and study files; perform quality assurance on study files; track and enter regulatory submissions; respond to queries and adverse events; screen and recruit clinical trial patients; follow up with patients to ensure protocol compliance.
Seniority
Individual Contributor